The DOI matches its Crossref record; 39 of the 39 references it cites were found in a registry or an index.
IL-33, the IL-1-like cytokine ligand for ST2 receptor, is a chromatin-associated nuclear factor in vivo
Open accessAbstract
Recent studies indicate that IL-1α functions intracellularly in pathways independent of its cell surface receptors by translocating to the nucleus and regulating transcription. Similarly, the chromatin-associated protein HMGB1 acts as both a nuclear factor and a secreted proinflammatory cytokine. Here, we show that IL-33, an IL-1-like cytokine that signals via the IL-1 receptor-related protein ST2 and induces T helper type 2-associated cytokines, is an endothelium-derived, chromatin-associated nuclear factor with transcriptional repressor properties. We found that IL-33 is identical to NF-HEV, a nuclear factor preferentially expressed in high endothelial venules (HEV), that we previously characterized. Accordingly, in situ hybridization demonstrated that endothelial cells constitute a major source of IL-33 mRNA in chronically inflamed tissues from patients with rheumatoid arthritis and Crohn's disease. Immunostaining with three distinct antisera, directed against the N-terminal part and IL-1-like C-terminal domain, revealed that IL-33 is a heterochromatin-associated nuclear factor in HEV endothelial cells in vivo . Association of IL-33 with heterochromatin was also observed in human and mouse cells under living conditions. In addition, colocalization of IL-33 with mitotic chromatin was noted. Nuclear localization, heterochromatin-association, and targeting to mitotic chromosomes were all found to be mediated by an evolutionarily conserved homeodomain-like helix–turn–helix motif within the IL-33 N-terminal part. Finally, IL-33 was found to possess transcriptional repressor properties, associated with the homeodomain-like helix–turn–helix motif. Together, these data suggest that, similarly to IL1α and HMGB1, IL-33 is a dual function protein that may function as both a proinflammatory cytokine and an intracellular nuclear factor with transcriptional regulatory properties.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“IL-33 is highly expressed within endothelial cells in the synovium of patients with rheumatoid arthritis87, and IL-33-deficient mice have reduced neutrophil migration in an experimental model of rheumatoid arthritis88, but the actual role of this cytokine in the pathogenesis of rheumatoid arthritis or other sterile inflammatory diseases remains to be determined.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [87]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Biologic basis for interleukin-1 in disease.
Dinarello, C. (1996) · Blood · doi:10.1182/blood.v87.6.2095.bloodjournal8762095 · Cited by 4,344
Release of chromatin protein HMGB1 by necrotic cells triggers inflammation
Scaffidi, P., Misteli, T., & Bianchi, M. E. (2002) · Nature · doi:10.1038/nature00858 · Cited by 4,221
Schmitz, J., Owyang, A. M., Oldham, E. R., Song, Y., Murphy, E., McClanahan, T. K., Zurawski, G., Moshrefi, M., Qin, J., Li, X., et al. (2005) · Immunity · doi:10.1016/j.immuni.2005.09.015 · Cited by 3,773
HMG-1 as a Late Mediator of Endotoxin Lethality in Mice
Wang, H., Bloom, O., Zhang, M., Vishnubhakat, J. M., Ombrellino, M., Che, J., Frazier, A., Yang, H., Ivanova, S., Borovikova, L. V., et al. (1999) · Science · doi:10.1126/science.285.5425.248 · Cited by 3,386
Yang, Y., Li, S., Yang, Q., Shi, Y., Zheng, M., Liu, Y., Chen, F., Song, G., Xu, H., Wan, T., et al. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000358696 · Cited by 3,263
High-mobility group box 1 protein (HMGB1): nuclear weapon in the immune arsenal
Lotze, M. T., & Tracey, K. J. (2005) · Nature reviews. Immunology · doi:10.1038/nri1594 · Cited by 2,490
Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion
Bonaldi, T., Talamo, F., Scaffidi, P., Ferrera, D., Porto, A., Bachi, A., Rubartelli, A., Agresti, A., & Bianchi, M. E. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg516 · Cited by 1,252
Association of transcriptionally silent genes with Ikaros complexes at centromeric heterochromatin.
Brown, K., Guest, S. S., Smale, S., Hahm, K., Merkenschlager, M., & Fisher, A. (1997) · Cell · doi:10.1016/s0092-8674(00)80472-9 · Cited by 824
HMG1 and 2, and related ‘architectural’ DNA-binding proteins
Thomas, J. O., & TRAVERS, A. A. (2001) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(01)01801-1 · Cited by 619
Ikaros DNA-Binding Proteins Direct Formation of Chromatin Remodeling Complexes in Lymphocytes
Kim, J., Sif, S., Jones, B., Jackson, A., Koipally, J., Heller, E., Winandy, S., Viel, A., Sawyer, A., Ikeda, T., et al. (1999) · Immunity · doi:10.1016/s1074-7613(00)80034-5 · Cited by 587
Research works printed but not linked: 1
- CA Dinarello Eur Cytokine Netw 11, 483–486 (2000).
Cited by
Sorted by citations
Items 101–200 of 965
A critical role of IL-33 in experimental allergic rhinitis
Haenuki, Y., Matsushita, K., Futatsugi-Yumikura, S., Ishii, K. J., Kawagoe, T., Imoto, Y., Fujieda, S., Yasuda, M., Hisa, Y., Akira, S., et al. (2012) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.02.013 · Cited by 233
IL-33 Is Produced by Mast Cells and Regulates IgE-Dependent Inflammation
Hsu, C., Neilsen, C. V., & Bryce, P. J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011944 · Cited by 242
Salker, M. S., Nautiyal, J., Steel, J. H., Webster, Z., Šućurović, S., Nicou, M., Singh, Y., Lucas, E. S., Murakami, K., Chan, Y., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052252 · Cited by 228
Production and functions of IL-33 in the central nervous system
Yasuoka, S., Kawanokuchi, J., Parajuli, B., Jin, S., Doi, Y., Noda, M., Sonobe, Y., Takeuchi, H., Mizuno, T., & Suzumura, A. (2011) · Brain Research · doi:10.1016/j.brainres.2011.02.045 · Cited by 222
Küchler, A. M., Pollheimer, J., Balogh, J., Sponheim, J., Manley, L., Sørensen, D. R., Angelis, P. M. D., Scott, H., & Haraldsen, G. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.080014 · Cited by 221
Kim, B., Lee, Y. M., Kim, E., Kwak, A., Ryoo, S., Bae, S. H., Azam, T., Kim, S., & Dinarello, C. A. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00391 · Cited by 231
Suppression of innate inflammation and immunity by interleukin‐37
Dinarello, C. A., Nold‐Petry, C. A., Nold, M. F., Fujita, M., Li, S., Kim, S., & Bufler, P. (2016) · European Journal of Immunology · doi:10.1002/eji.201545828 · Cited by 218
IL-33 Induces IL-13–Dependent Cutaneous Fibrosis
Rankin, A. L., Mumm, J. B., Murphy, E., Turner, S. P., Yu, N., McClanahan, T. K., Bourne, P. A., Pierce, R. H., KASTELEIN, R. A., & Pflanz, S. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0903306 · Cited by 222
Cytokine-Induced Modulation of Colorectal Cancer
Mager, L. F., Wasmer, M.-H., Rau, T. T., & Krebs, P. (2016) · Frontiers in Oncology · doi:10.3389/fonc.2016.00096 · Cited by 223
Danger Signals Activating the Immune Response after Trauma
Hirsiger, S., Simmen, H., Werner, C. M. L., Wanner, G. A., & Rittirsch, D. (2012) · Mediators of Inflammation · doi:10.1155/2012/315941 · Cited by 216
Induction of IL-33 expression and activity in central nervous system glia
Hudson, C. A., Christophi, G. P., Gruber, R. C., Wilmore, J. R., Lawrence, D. A., & Massa, P. T. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.1207830 · Cited by 213
Damage-associated molecular patterns in trauma
Relja, B., & Land, W. G. (2019) · European Journal of Trauma and Emergency Surgery · doi:10.1007/s00068-019-01235-w · Cited by 225
Sedhom, M. A. K., Pichery, M., Murdoch, J. R., Foligné, B., Ortéga, N., Normand, S., Mertz, K. D., Sanmugalingam, D., Brault, L., Grandjean, T., et al. (2012) · Gut · doi:10.1136/gutjnl-2011-301785 · Cited by 211
Self-citationInflammation in acute and chronic pancreatitis
Habtezion, A. (2015) · Current Opinion in Gastroenterology · doi:10.1097/mog.0000000000000195 · Cited by 210
High endothelial venules (HEVs) in immunity, inflammation and cancer
Blanchard, L., & Girard, J. (2021) · Angiogenesis · doi:10.1007/s10456-021-09792-8 · Cited by 231
Self-citationInterleukin-33 enhances adhesion, CD11b expression and survival in human eosinophils
Suzukawa, M., Koketsu, R., Iikura, M., Nakae, S., Matsumoto, K., Nagase, H., Saito, H., Matsushima, K., Ohta, K., Yamamoto, K., et al. (2008) · Laboratory Investigation · doi:10.1038/labinvest.2008.82 · Cited by 206
Interleukin-33 biology with potential insights into human diseases
Palmer, G., & Gabay, C. (2011) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2011.53 · Cited by 214
IL‐33: a tissue derived cytokine pathway involved in allergic inflammation and asthma
Smith, D. E. (2009) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2009.03384.x · Cited by 211
IL-33 and IL-33 Receptors in Host Defense and Diseases
Oboki, K., Ohno, T., Kajiwara, N., Saito, H., & Nakae, S. (2010) · Allergology International · doi:10.2332/allergolint.10-rai-0186 · Cited by 210
Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease
Chapuis, J., Hot, D., Hansmannel, F., Kerdraon, O., Ferreira, S., Hubans, C., Maurage, C. A., Huot, L., Bensemain, F., Laumet, G., et al. (2009) · Molecular Psychiatry · doi:10.1038/mp.2009.10 · Cited by 201
Positive regulators of osteoclastogenesis and bone resorption in rheumatoid arthritis
Braun, T., & Zwerina, J. (2011) · Arthritis Research & Therapy · doi:10.1186/ar3380 · Cited by 208
The role of IL‐33 and mast cells in allergy and inflammation
Saluja, R., Khan, M., Church, M. K., & Maurer, M. (2015) · Clinical and Translational Allergy · doi:10.1186/s13601-015-0076-5 · Cited by 205
Overview of the interleukin-1 family of ligands and receptors
Dinarello, C. A. (2013) · Seminars in Immunology · doi:10.1016/j.smim.2013.10.001 · Cited by 198
Wills-Karp, M. A., Rani, R., Dienger, K. M., Lewkowich, I. P., Fox, J. G., Perkins, C. L., Lewis, L., Finkelman, F. D., Smith, D. E., Bryce, P. J., et al. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20110079 · Cited by 187
Koop, K., Backert, I., Wirtz, S. J., Hueber, A. J., Schett, G. A., Vieth, M. W., Probst, H. C., Bopp, T., Neurath, M. F., & Neufert, C. F. (2016) · Gut · doi:10.1136/gutjnl-2015-310374 · Cited by 192
Yang, Y., Andersson, P., Hosaka, K., Zhang, Y., Cao, R., Iwamoto, H., Yang, X., Nakamura, M., Wang, J., Zhuang, R., et al. (2016) · Nature Communications · doi:10.1038/ncomms11385 · Cited by 189
IL-33 Reduces Macrophage Foam Cell Formation
McLaren, J. E., Michael, D. R., Salter, R. C., Ashlin, T. G., Calder, C. J., Miller, A. M., Liew, F. Y., & Ramji, D. P. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000520 · Cited by 186
IL-33, a recently identified interleukin-1 gene family member, is expressed in human adipocytes
Wood, I. S., Wang, B., & Trayhurn, P. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.04.081 · Cited by 187
Palmer, G., Lipsky, B. P., Smithgall, M. D., Meininger, D. P., Siu, S., Talabot‐Ayer, D., Gabay, C., & Smith, D. E. (2008) · Cytokine · doi:10.1016/j.cyto.2008.03.008 · Cited by 181
Rider, P., Voronov, E., Dinarello, C. A., Apte, R. N., & Cohen, I. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601342 · Cited by 186
Boeck, A. D., Ahn, B. Y., D’Mello, C., Lun, X. Q., Menon, S. V., Alshehri, M. M., Szulzewsky, F., Shen, Y., Khan, L., Dang, N. H., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18569-4 · Cited by 191
IL-33 in T Cell Differentiation, Function, and Immune Homeostasis
Peine, C., Marek, R. M., & Löhning, M. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.03.007 · Cited by 187
Decoding asthma: Translating genetic variation in IL33 and IL1RL1 into disease pathophysiology
Grotenboer, N. S., Ketelaar, M. E., Koppelman, G. H., & Nawijn, M. C. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.11.028 · Cited by 182
Kenney, M. C., Chwa, M., Atilano, S. R., Falatoonzadeh, P., Ramírez, C., Malik, D., Tarek, M., Cáceres‐del‐Carpio, J., Nesburn, A. B., Boyer, D. S., et al. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.10.016 · Cited by 177
The IL-33/ST2 axis: Role in health and disease
la Fuente, M. D., MacDonald, T. T., & Hermoso, M. A. (2015) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2015.07.017 · Cited by 171
Sattler, S., Ling, G., Xu, D., Hussaarts, L., Romaine, A., Zhao, H., Fossati‐Jimack, L., Malik, T. H., Cook, H. T., Botto, M., et al. (2014) · Journal of Autoimmunity · doi:10.1016/j.jaut.2014.01.032 · Cited by 187
Mok, M. Y., Huang, F., Ip, W., Lo, Y., Wong, F. Y., Chan, E. Y. T., Lam, K. F., & Xu, D. (2009) · Lara D. Veeken · doi:10.1093/rheumatology/kep402 · Cited by 172
IL-1 family cytokines trigger sterile inflammatory disease
Lukens, J. R., Gross, J. M., & Kanneganti, T. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00315 · Cited by 178
Ozone exposure induces respiratory barrier biphasic injury and inflammation controlled by IL-33
Michaudel, C., Mackowiak, C., Maillet, I., Fauconnier, L., Akdiş, C. A., Sokołowska, M., Dreher, A., Tan, H. T., Quesniaux, V. F. J., Ryffel, B., et al. (2018) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.11.044 · Cited by 172
The IL-33/ST2 axis augments effector T-cell responses during acute GVHD
Reichenbach, D. K., Schwarze, V., Matta, B. M., Tkachev, V., Lieberknecht, E., Liu, Q., Koehn, B. H., Pfeifer, D., Taylor, P. A., Prinz, G., et al. (2015) · Blood · doi:10.1182/blood-2014-10-606830 · Cited by 173
Altered subcellular localization of IL-33 leads to non-resolving lethal inflammation
Bessa, J., Meyer, C. A., Mudry, M. C. D. V., Schlicht, S., Smith, S. H., Iglesias, A. H., & Cote-Sierra, J. (2014) · Journal of Autoimmunity · doi:10.1016/j.jaut.2014.02.012 · Cited by 182
Respiratory Syncytial Virus Disease Is Mediated by Age-Variable IL-33
Saravia, J., You, D., Shrestha, B., Jaligama, S., Siefker, D. T., Lee, G. I., Harding, J. N., Jones, T. L., Rovnaghi, C. R., Bagga, B., et al. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005217 · Cited by 170
Matsuyama, Y., Okazaki, H., Tamemoto, H., KIMURA, H., Kamata, Y., Nagatani, K., Nagashima, T., Hayakawa, M., Iwamoto, M., Yoshio, T., et al. (2009) · The Journal of Rheumatology · doi:10.3899/jrheum.090492 · Cited by 169
New Cytokines in the Pathogenesis of Atopic Dermatitis—New Therapeutic Targets
Klonowska, J., Gleń, J., Nowicki, R. J., & Trzeciak, M. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103086 · Cited by 174
IL‐33 induces skin inflammation with mast cell and neutrophil activation
Hueber, A. J., Alves-Filho, J. C., Asquith, D. L., Michels, C., Millar, N. L., Reilly, J. H., Graham, G. J., Liew, F. Y., Miller, A. M., & McInnes, I. B. (2011) · European Journal of Immunology · doi:10.1002/eji.201041360 · Cited by 169
The IL-33/ST2 pathway — A new therapeutic target in cardiovascular disease
Miller, A. M., & Liew, F. Y. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.02.005 · Cited by 168
Demyanets, S., Kaun, C., Pentz, R., Krychtiuk, K. A., Rauscher, S., Pfaffenberger, S., Zuckermann, A. O., Aliabadi, A. Z., Gröger, M., Maurer, G., et al. (2013) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2013.03.020 · Cited by 168
New Insights in the Immunobiology of IL-1 Family Members
van de Veerdonk, F. L., & Netea, M. G. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00167 · Cited by 170
Hoshino, T., Okamoto, M., Sakazaki, Y., Kato, S., Young, H. A., & Aizawa, H. (2009) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2008-0182oc · Cited by 164
Epithelial-Derived Cytokines in Asthma
Mitchell, P. D., & O’Byrne, P. M. (2016) · CHEST Journal · doi:10.1016/j.chest.2016.10.042 · Cited by 171
Cytokine inhibition in the treatment of COPD
Chung, K. F., Caramori, G., Adcock, I. M., & Stefano, A. D. (2014) · International Journal of COPD · doi:10.2147/copd.s42544 · Cited by 173
IL-33 Exacerbates Acute Kidney Injury
Akçay, A., Nguyen, Q., He, Z., Türkmen, K., Lee, D. W., Andrés-Hernando, A., Altmann, C. J., Toker, A., Pačić, A., Ljubanović, D. G., et al. (2011) · Journal of the American Society of Nephrology · doi:10.1681/asn.2010091011 · Cited by 166
Yazdi, A. S., & Ghoreschi, K. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-94-024-0921-5_2 · Cited by 174
Myocardial pressure overload induces systemic inflammation through endothelial cell IL-33
Chen, W., Hong, J., Gannon, J., Kakkar, R. K., & Lee, R. T. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1424236112 · Cited by 162
Interleukin-33 and the function of innate lymphoid cells
Mirchandani, A. S., Salmond, R. J., & Liew, F. Y. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.04.005 · Cited by 164
Caspase-1, Caspase-8, and Calpain Are Dispensable for IL-33 Release by Macrophages
Ohno, T., Oboki, K., Kajiwara, N., Morii, E., Aozasa, K., Flavell, R. A., Okumura, K., Saito, H., & Nakae, S. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802449 · Cited by 160
Regulation and Function of the IL-1 Family Cytokine IL-1F9 in Human Bronchial Epithelial Cells
Chustz, R. T., Nagarkar, D. R., Poposki, J. A., Favoreto, S., Avila, P. C., Schleimer, R. P., & Kato, A. (2010) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2010-0075oc · Cited by 157
Rider, P., Carmi, Y., Voronov, E., & Apte, R. N. (2013) · Seminars in Immunology · doi:10.1016/j.smim.2013.10.005 · Cited by 155
IL-33 activates tumor stroma to promote intestinal polyposis
Maywald, R. L., Doerner, S. K., Pastorelli, L., Salvo, C. D., Benton, S. M., Dawson, E. P., Lanza, D. G., Berger, N. A., Markowitz, S. D., Lenz, H., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1422445112 · Cited by 159
Alternative splicing of interleukin-33 and type 2 inflammation in asthma
Gordon, E. D., Simpson, L. J., Rios, C. L., Ringel, L., Lachowicz-Scroggins, M. E., Peters, M. C., Wesolowska‐Andersen, A., Gonzalez, J. R., MacLeod, H. J., Christian, L. S., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1601914113 · Cited by 160
Type 2 innate immune responses and the natural helper cell
Koyasu, S., & Moro, K. (2011) · Immunology · doi:10.1111/j.1365-2567.2011.03413.x · Cited by 155
Demyanets, S., Kónya, V., Kastl, S., Kaun, C., Rauscher, S., Niessner, A., Pentz, R., Pfaffenberger, S., Rychli, K., Lemberger, C. E., et al. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.231431 · Cited by 156
Chen, S.-F., Nieh, S., Jao, S., Wu, M.-Z., Liu, C., Chang, Y., & Lin, Y. (2013) · The Journal of Pathology · doi:10.1002/path.4226 · Cited by 152
Espinassous, Q., Paco, E. G. D., García-Verdugo, I., Synguélakis, M., von Aulock, S., Sallenave, J., McKenzie, A. N. J., & Kanellopoulos, J. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803067 · Cited by 158
Soluble ST2: A complex and diverse role in several diseases
Homšak, E., & Gruson, D. (2020) · Clinica Chimica Acta · doi:10.1016/j.cca.2020.04.011 · Cited by 151
Sponheim, J., Pollheimer, J., Olsen, T., Balogh, J., Hammarström, C. L., Loos, T., Kasprzycka, M., Sørensen, D. R., Nilsen, H. R., Küchler, A. M., et al. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.100378 · Cited by 158
Alarmin IL-33 Acts as an Immunoadjuvant to Enhance Antigen-Specific Tumor Immunity
Villarreal, D. O., Wise, M. C., Walters, J. N., Reuschel, E. L., Choi, M. J., Obeng-Adjei, N., Yan, J., Morrow, M. P., & Weiner, D. B. (2014) · Cancer Research · doi:10.1158/0008-5472.can-13-2729 · Cited by 147
The central role of IL-33/IL-1RL1 pathway in asthma: From pathogenesis to intervention
Jayalatha, A. K. S., Hesse, L., Ketelaar, M. E., Koppelman, G. H., & Nawijn, M. C. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107847 · Cited by 150
Schneider, E., Petit-Bertron, A.-F., Rignault‐Bricard, R., Levasseur, M., Ramadan, A., Girard, J., Herbelin, A., & Dy, M. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900328 · Cited by 152
Self-citationPomeshchik, Y., Kidin, I., Korhonen, P., Savchenko, E., Jaronen, M., Lehtonen, Š., Wojciechowski, S., Kanninen, K. M., Koıstınaho, J., & Malm, T. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.08.002 · Cited by 143
Schulze, J., Bickert, T., Beil, F. T., Zaiss, M. M., Albers, J., Wintges, K., Streichert, T., Klaetschke, K., Keller, J., Hißnauer, T.-N., et al. (2010) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.269 · Cited by 146
Hristova, M., Habibovic, A., Veith, C., Janssen-Heininger, Y. M. W., Dixon, A. E., Geiszt, M., & van der Vliet, A. (2016) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2015.10.003 · Cited by 141
A network map of IL-33 signaling pathway
Pinto, S. M., Subbannayya, Y., Balaya, R. D. A., Raju, R., Chatterjee, O., Advani, J., Radhakrishnan, A., Prasad, T. S. K., Wani, M. R., & Pandey, A. (2018) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-018-0464-4 · Cited by 141
Sounding the alarmins—The role of alarmin cytokines in asthma
Gauvreau, G. M., Bergeron, C., Boulet, L., Cockcroft, D. W., Côté, A., Davis, B. E., Leigh, R., Myers, I., O’Byrne, P. M., & Sehmi, R. (2022) · Allergy · doi:10.1111/all.15609 · Cited by 154
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma
Smith, D. E., Helgason, H., Sulem, P., Björnsdóttir, U. S., Lim, A. C., Sveinbjörnsson, G., Hasegawa, H., Brown, M. E., Ketchem, R. R., Gavala, M. L., et al. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006659 · Cited by 140
Immunomodulation by interleukin-33 is protective in stroke through modulation of inflammation
Korhonen, P., Kanninen, K. M., Lehtonen, Š., Lemarchant, S., Puttonen, K. A., Oksanen, M., Dhungana, H., Loppi, S. H., Pollari, E., Wojciechowski, S., et al. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.06.013 · Cited by 141
A signalling cascade of IL-33 to IL-13 regulates metaplasia in the mouse stomach
Petersen, C. P., Meyer, A. R., Salvo, C. D., Choi, E.-Y. K., Schlegel, C. E., Petersen, A., Engevik, A. C., Prasad, N., Levy, S., Peebles, R. S., et al. (2017) · Gut · doi:10.1136/gutjnl-2016-312779 · Cited by 139
Expression and regulation of interleukin‐33 in human monocytes
Nile, C. J., Barksby, E., Jitprasertwong, P., Preshaw, P. M., & Taylor, J. J. (2010) · Immunology · doi:10.1111/j.1365-2567.2009.03221.x · Cited by 145
Injury, repair, inflammation and metaplasia in the stomach
Meyer, A. R., & Goldenring, J. R. (2018) · The Journal of Physiology · doi:10.1113/jp275512 · Cited by 136
Zhou, Q., Wu, X., Wang, X., Yu, Z., Pan, T., Li, Z., Chang, X., Jin, Z., Li, J., Zhu, Z., et al. (2019) · Oncogene · doi:10.1038/s41388-019-1078-x · Cited by 135
Satsutani, N. M., Ito, T., Nakanishi, T., Inagaki, N., Tanaka, A., Vien, P. T. X., Kibata, K., Inaba, M., & Nomura, S. (2014) · Allergology International · doi:10.2332/allergolint.13-oa-0672 · Cited by 138
Interleukin-33 contributes to both M1 and M2 chemokine marker expression in human macrophages
Joshi, A., Oak, S. R., Hartigan, A. J., Finn, W. G., Kunkel, S. L., Duffy, K. E., Das, A., & Hogaboam, C. M. (2010) · BMC Immunology · doi:10.1186/1471-2172-11-52 · Cited by 140
An intrinsic role of IL-33 in Treg cell–mediated tumor immunoevasion
Hatzioannou, A., Banos, A., Sakellaropoulos, T., Fedonidis, C., Vidali, M.-S., Köhne, M., Händler, K., Boon, L., Henriques, A. R., Koliaraki, V., et al. (2019) · Nature Immunology · doi:10.1038/s41590-019-0555-2 · Cited by 135
Opposing Functions of Classic and Novel IL-1 Family Members in Gut Health and Disease
Lopetuso, L. R., Chowdhry, S., & Pizarro, T. T. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00181 · Cited by 139
Biology of IL-36 Signaling and Its Role in Systemic Inflammatory Diseases
Yuan, Z., Xu, W., Liu, X.-Y., Liu, X., Huang, A., & Su, L. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02532 · Cited by 134
Gao, K., Li, X., Zhang, L., Bai, L., Dong, W., Gao, K., Shi, G., Xia, X., Wu, L., & Zhang, L. (2013) · Cancer Letters · doi:10.1016/j.canlet.2013.03.002 · Cited by 135
Infection with Influenza Virus Induces IL-33 in Murine Lungs
Goffic, R. L., Arshad, M. I., Rauch, M., L’Helgoualc’h, A., Delmas, B., Piquet‐Pellorce, C., & Samson, M. (2011) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2010-0516oc · Cited by 141
Cellular context of IL-33 expression dictates impact on anti-helminth immunity
Hung, L., Tanaka, Y., Herbine, K., Pastore, C., Singh, B. K., Ferguson, A. A., Vora, N., Douglas, B. B., Zullo, K. M., Behrens, E. M., et al. (2020) · Science Immunology · doi:10.1126/sciimmunol.abc6259 · Cited by 131
Nuclear IL-33 is a transcriptional regulator of NF-κB p65 and induces endothelial cell activation
Choi, Y.-S., Park, J. A., Kim, J., Rho, S.-S., Park, H., Kim, Y., & Kwon, Y. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.04.005 · Cited by 137
Cheng, W., Shivshankar, P., Li, Z., Chen, L., Yeh, I., & Zhong, G. (2007) · Infection and Immunity · doi:10.1128/iai.01064-07 · Cited by 128
The biological paths of IL-1 family members IL-18 and IL-33
Smith, D. E. (2010) · Journal of Leukocyte Biology · doi:10.1189/jlb.0810470 · Cited by 128
England, E., Rees, D. G., Scott, I. C., Carmen, S., Chan, D. T. Y., Chaillan, C., Houslay, K. F., Erngren, T., Penney, M., Majithiya, J. B., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-36642-y · Cited by 127
Serum Interleukin-33 Levels in Patients with Gastric Cancer
Sun, P., Ben, Q., Tu, S., Dong, W., Qi, X., & Wu, Y. (2011) · Digestive Diseases and Sciences · doi:10.1007/s10620-011-1760-5 · Cited by 130
The Pleiotropic Immunomodulatory Functions of IL-33 and Its Implications in Tumor Immunity
Afferni, C., Buccione, C., Andreone, S., Galdiero, M. R., Varricchi, G., Marone, G., Mattei, F., & Schiavoni, G. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02601 · Cited by 126
Byrne, S. N., Beaugie, C., O’Sullivan, C., Leighton, S., & Halliday, G. M. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.03.010 · Cited by 124
Immunity to gastrointestinal nematode infections
Sorobetea, D., Svensson, M., & Grencis, R. K. (2018) · Mucosal Immunology · doi:10.1038/mi.2017.113 · Cited by 122
Role of IL-33-ST2 pathway in regulating inflammation: current evidence and future perspectives
Zhou, Y., Xu, Z., & Liu, Z. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04782-4 · Cited by 136
Ivanov, V. N., Zhou, H., Ghandhi, S. A., Karasic, T. B., Yaghoubian, B., Amundson, S. A., & Hei, T. K. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2010.02.010 · Cited by 128
Meephansan, J., Tsuda, H., Komine, M., Tominaga, S., & Ohtsuki, M. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.185 · Cited by 127
Gabryelska, A., Kuna, P., Antczak, A. J., Białasiewicz, P., & Panek, M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00692 · Cited by 121
Metadata
- Authors
- Carriere, V., Roussel, L., Ortega, N., Lacorre, D.-A., Americh, L., Aguilar, L., Bouche, G., & Girard, J.-P.
- Affiliations
- *Laboratoire de Biologie Vasculaire, Equipe Labellisée “La Ligue 2006,” Institut de Pharmacologie et de Biologie Structurale, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5089, 205 Route de Narbonne, 31077 Toulouse, France; and
- Centre National de la Recherche Scientifique (FR)
- Endocube, Prologue Biotech, BP700, Rue Pierre et Marie Curie, 31319 Labège Cedex, France
- Corresponding author
- Girard, Jean-Philippe
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2007-01-02
- Volume
- 104
- Issue
- 1
- Pages
- 282-287
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1765450
- OpenAlex
- W2093396768
- Cited by
- 966
- References
- 38
- Citations by year
- 2026: 20 · 2025: 29 · 2024: 30 · 2023: 49 · 2022: 50 · 2021: 51 · 2020: 47 · 2019: 51 · 2018: 58 · 2017: 55 · 2016: 64 · 2015: 70 · 2014: 52 · 2013: 56 · 2012: 72
- FWCI
- 12.14
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Association pour la Recherche sur le Cancer
- Drug Applied Research Center, Tabriz University of Medical Sciences
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- IL-33, ST2 receptor, heterochromatin, nuclear factors, transcriptional repressor, endothelial cells, high endothelial venules, rheumatoid arthritis, Crohn's disease, chronic inflammation, HMGB1
- MeSH terms
- Interleukin-33, Interleukin-1 Receptor-Like 1 Protein, Animals, Arthritis, Rheumatoid, Crohn Disease, HeLa Cells, Heterochromatin, Humans, Interleukins, Membrane Proteins, Mitosis, Nuclear Proteins, Receptors, Cell Surface, Repressor Proteins, RNA, Messenger, 3T3 Cells, Conserved Sequence, Receptors, Interleukin, Nuclear Localization Signals, Amino Acid Motifs, Endothelial Cells, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review